Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1559414131 1.000 0.080 3 38709556 inframe deletion AGA/- delins 1
rs57326399 1.000 0.080 3 38726809 missense variant T/C snv 0.24 0.21 1
rs6599240 1.000 0.080 3 38697226 3 prime UTR variant G/A snv 0.44 1
rs6599257 1.000 0.080 3 38763097 intron variant C/T snv 0.74 1
rs7428167 1.000 0.080 3 38736700 intron variant T/C snv 0.59 1
rs7430439 1.000 0.080 3 38762148 intron variant G/A snv 0.66 1
rs7641844 1.000 0.080 3 38760760 intron variant A/G snv 0.33 0.31 1
rs774893568 1.000 0.080 3 38714013 missense variant C/T snv 4.4E-05 7.0E-05 1
rs9874633 1.000 0.080 3 38730503 intron variant A/G snv 0.38 1
rs267607028 0.925 0.080 19 35033827 stop gained G/A snv 8.0E-06 2
rs267607029 0.925 0.080 19 35033828 stop gained G/A snv 2
rs587777023 1.000 0.080 11 118166903 missense variant T/C snv 8.0E-06 2.1E-05 1
rs147205617 1.000 0.080 11 123642563 missense variant C/T snv 3.1E-04 3.1E-04 2
rs121918282 0.882 0.080 11 123653773 missense variant A/G snv 2.0E-04 3.5E-04 3
rs1064794243 0.851 0.200 17 63941169 missense variant A/T snv 5
rs1805124 0.742 0.280 3 38603929 missense variant T/C snv 0.22 0.25 16
rs137854618 0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06 15
rs45546039 0.732 0.120 3 38613781 missense variant C/A;T snv 4.1E-06 15
rs41261344 0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 11
rs137854601 0.776 0.120 3 38551022 stop gained C/A;T snv 4.0E-06 10
rs199473097 0.763 0.120 3 38606710 missense variant G/A snv 8.0E-06 7.0E-06 9
rs757532106 0.763 0.120 3 38550500 stop gained G/A snv 4.5E-05 4.9E-05 9
rs199473605 0.851 0.120 3 38560374 missense variant C/G;T snv 4.8E-05; 4.0E-06 7
rs11708996 0.925 0.120 3 38592432 intron variant G/C snv 0.11 6
rs137854600 0.807 0.120 3 38551504 missense variant C/A;T snv 6